JP2015140399A - Ink composition for inkjet recording - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a nonaqueous ink composition for inkjet recording which is excellent in storage stability while improving abrasion resistance of a recorded image.SOLUTION: The nonaqueous ink composition for inkjet recording according to the present invention contains: a pigment; a compound represented by general formula (1); and a phthalocyanine derivative into which a polar group having no amine structure has been introduced, as a pigment dispersant for dispersing the pigment. Preferably, the pigment is carbon black. Preferably, the nonaqueous ink composition for inkjet recording further contains an alkylene glycol monoalkyl ether. (In the general formula (1), Rrepresents a C1-C4 alkyl group, and Rand Reach independently represent a methyl group or an ethyl group.)

Description

  The present invention relates to an ink composition for ink jet recording.

  2. Related Art Inkjet recording apparatuses that record images and characters by ejecting minute droplets of an ink composition from nozzle holes of a recording head and attaching them to a recording medium are known. As an ink composition used for such recording, an aqueous (aqueous) ink composition in which a pigment, a pigment dispersant, a resin or the like is dispersed or dissolved in water is known. Furthermore, a non-aqueous (oil-based) ink composition in which pigments, pigment dispersants, resins and the like are dispersed or dissolved in an organic solvent without containing water has been developed.

  Among the inks described above, the non-aqueous ink composition has good ink wettability with respect to a recording medium having a recording surface of plastic (for example, vinyl chloride, polyester, polypropylene, polyethylene, etc.) It has been widely used because of its good ink fixing property. For example, Patent Document 1 discloses a non-aqueous ink composition for inkjet recording containing an amide solvent (ether amides).

  In addition, a non-aqueous ink composition may contain a pigment dispersant such as a resin dispersant or a pigment derivative (synergist) in order to improve the dispersibility of the pigment and enhance the storage stability of the ink. . For example, Patent Document 2 describes the use of a pigment dispersion resin, a pigment derivative having a phthalocyanine skeleton, and the like.

JP 2013-155275 A JP 2012-219131 A

  A pigment derivative as described in Patent Document 2 has a property of being easily dissolved in an organic solvent while having a property of being hardly dissolved in water. Therefore, the pigment derivative tends to exist in a state where it is separated from the pigment in the ink and eluted in the solvent. In particular, when the amide solvent described in Patent Document 1 is used, the pigment derivative is easily eluted into the solvent.

  However, although the amide solvent described in Patent Document 1 has the advantage of being excellent in fixability and drying of recorded images as compared with other organic solvents (for example, lactones, glycol ethers, and the like), it absorbs water. It has the property of being high. Then, when a non-aqueous ink composition containing an amide solvent and a pigment derivative is stored for a long period of time, the pigment derivative eluted in the solvent becomes difficult to dissolve in the ink having a high water content, and precipitates as a foreign matter. A malfunction occurs. That is, foreign matters derived from pigment derivatives tend to be remarkably generated when an amide solvent is used in combination.

  As described above, it has been difficult to obtain an ink excellent in storage stability with less generation of foreign matters and less change in viscosity while improving the rubbing resistance (fixability) of the recorded image.

Some embodiments according to the present invention provide a non-aqueous ink composition for ink-jet recording which has improved storage stability while solving at least a part of the above-described problems and has excellent storage stability. To provide things.

  SUMMARY An advantage of some aspects of the invention is to solve at least a part of the problems described above, and the invention can be implemented as the following aspects or application examples.

[Application Example 1]
One aspect of the non-aqueous ink composition for ink jet recording according to the present invention is:
Pigments,
A compound represented by the following general formula (1):
As a pigment dispersant for dispersing the pigment, a phthalocyanine derivative into which a polar group having no amine structure is introduced,
Containing.

（上記一般式（１）中、Ｒ^１は、炭素数１以上４以下のアルキル基を示し、Ｒ^２およびＲ^３は、それぞれ独立に、メチル基またはエチル基を示す。）

(In the general formula (1), R ¹ represents an alkyl group having 1 to 4 carbon atoms, and R ² and R ³ each independently represent a methyl group or an ethyl group.)

[Application Example 2]
In application example 1,
The pigment may be carbon black.

[Application Example 3]
In application example 1 or application example 2,
Further, an alkylene glycol monoalkyl ether can be contained.

[Application Example 4]
In application example 3,
The content of the alkylene glycol monoalkyl ether may be 1% by mass or more and 40% by mass or less based on the total mass of the non-aqueous ink composition.

[Application Example 5]
In any one of Application Examples 1 to 4,
The content of the compound represented by the general formula (1) may be 5% by mass or more and 50% by mass or less with respect to the total mass of the non-aqueous ink composition.

[Application Example 6]
In any one of Application Examples 1 to 5,
Furthermore, at least one resin of a vinyl chloride resin and a (meth) acrylic resin can be contained.

[Application Example 7]
In Application Example 6,
The content of the resin may be 0.5% by mass or more and 10% by mass or less with respect to the total mass of the non-aqueous ink composition.

[Application Example 8]
In any one of the application examples 1 to 7,
The content of the phthalocyanine derivative may be 1 part by mass or more and 20 parts by mass or less with respect to 100 parts by mass of the pigment.

[Application Example 9]
In any one of Application Examples 1 to 8,
The pigment dispersant may further contain a compound other than the phthalocyanine derivative.

FIG. 2 is a perspective view schematically showing a configuration of an ink jet printer that can be used in the present embodiment.

  Several embodiments of the present invention will be described below. Embodiment described below demonstrates an example of this invention. The present invention is not limited to the following embodiments, and includes various modified embodiments that are implemented within a range that does not change the gist of the present invention. Note that not all of the configurations described below are essential configurations of the present invention.

  In the present invention, “image” refers to a print pattern formed from a group of dots, and includes text printing and solid printing.

  In the present invention, the “non-aqueous ink composition” is an ink composition in which an organic solvent is a main solvent and water is not a main solvent. Preferably, the content of water in the composition is 3% by mass or less, more preferably 1% by mass or less, still more preferably less than 0.05% by mass, still more preferably less than 0.01% by mass, More preferably, it means less than 0.005% by mass, and most preferably less than 0.001% by mass. Or it is good also as an ink composition which does not contain water substantially. “Substantially not containing” means not intentionally containing.

1. Non-aqueous ink composition A non-aqueous ink composition for ink jet recording according to an embodiment of the present invention (hereinafter, also simply referred to as “non-aqueous ink composition”) is represented by a pigment and the following general formula (1). And a phthalocyanine derivative introduced with a polar group having no amine structure as a pigment dispersant for dispersing the pigment. The compound represented by the following general formula (1) is an organic solvent that functions as a solvent for the non-aqueous ink composition.

Hereinafter, components included in the non-aqueous ink composition for inkjet recording according to the present embodiment and components that can be included will be described in detail.

1.1. Pigment The non-aqueous ink composition according to this embodiment contains a pigment. Examples of the pigment include inorganic pigments and organic pigments.

Among the pigments, examples of the inorganic pigment include carbon black, iron oxide, and titanium oxide. Although it does not specifically limit as said carbon black, For example, furnace black, lamp black, acetylene black, and channel black (CI pigment black 7) are mentioned. Further, as a commercially available product of carbon black, for example, No. 2300, 900, MCF88, no. 20B, no. 33, no. 40, no. 45, no. 52, MA7, MA8, MA100, no. 2200B (all trade names, manufactured by Mitsubishi Chemical Corporation), color black FW1, FW2, FW2V, FW18, FW200, S150, S160, S170, Pretex 35, U, V, 140U, Special Black 6, 5, 4A, 4, 250 (all trade names, manufactured by Degussa AG), CONDUCTEX SC, Raven 1255, 5750, 5250, 5000, 3500, 1255, 700 (all trade names, Columbia Carbon ( Columbian Carbon Japan Ltd), Columbian Chemicals, Regal 400R, 330R, 660R, Mogul L, Monarch 700, 800, 880, 900, 1000, 1100, 1300, 1400, Elftex 12 (all above) Product name, Cabot Corporation)).

  Examples of organic pigments include quinacridone pigments, quinacridone quinone pigments, dioxazine pigments, phthalocyanine pigments, anthrapyrimidine pigments, anthanthrone pigments, indanthrone pigments, flavanthrone pigments, perylene pigments, diene pigments. Examples include ketopyrrolopyrrole pigments, perinone pigments, quinophthalone pigments, anthraquinone pigments, thioindigo pigments, benzimidazolone pigments, isoindolinone pigments, azomethine pigments, and azo pigments.

  Among the above-mentioned pigments, at least one of carbon black and phthalocyanine pigment is used from the viewpoint of excellent dispersibility when a phthalocyanine derivative (described later) used in the non-aqueous ink composition according to this embodiment is used. It is preferable.

  Here, when a phthalocyanine pigment is used as the pigment, the phthalocyanine derivative is unlikely to be detached from the phthalocyanine pigment because the pigment and the phthalocyanine derivative have a common structure (phthalocyanine skeleton). On the other hand, since carbon black does not have a phthalocyanine structure skeleton, the phthalocyanine derivative is easily detached from the carbon black. The detached phthalocyanine derivative is easily converted into a foreign substance in the ink whose water content is increased by the water absorption action of the solvent. However, according to the non-aqueous ink composition according to the present embodiment, since a phthalocyanine derivative having a specific structure (described later) is used, even when the phthalocyanine derivative is detached from the pigment, the problem of foreign matter formation hardly occurs. . As described above, the non-aqueous ink composition according to this embodiment can exert its effect well even when carbon black is used as a pigment.

  The content of the pigment can be appropriately set as desired and is not particularly limited. For example, the content of the pigment is 0.1% by mass with respect to the total mass (100% by mass) of the non-aqueous ink composition. The content may be 25% by mass or less, and may be 1% by mass or more and 10% by mass or less.

1.2. Organic solvent 1.2.1. Compound Represented by General Formula (1) The non-aqueous ink composition according to this embodiment contains a compound represented by the following general formula (1).

In the above formula (1), R ¹ represents an alkyl group having 1 to 4 carbon atoms, and R ² and R ³ each independently represent a methyl group or an ethyl group. The “alkyl group having 1 to 4 carbon atoms” may be a linear or branched alkyl group such as a methyl group, an ethyl group, an n-propyl group, an iso-propyl group, or an n-butyl group. , Sec-butyl group, iso-butyl group, and tert-butyl group. The compounds represented by the above formula (1) may be used singly or in combination of two or more.

  The function of the compound represented by the general formula (1) includes enhancing the surface drying property and the fixing property of the ink deposited on the recording medium having low ink absorption. In particular, the compound represented by the general formula (1) is excellent in the action of appropriately dissolving the vinyl chloride resin. Therefore, the compound represented by the general formula (1) can dissolve the recording surface containing the vinyl chloride resin and allow the ink to penetrate into the recording medium. As the ink penetrates into the recording medium in this way, the ink is firmly fixed and the surface of the ink is easily dried. Therefore, the obtained image has excellent surface drying and fixing properties (rubbing resistance).

  Since the compound represented by the general formula (1) has high water absorption (hygroscopicity) among organic solvents described later, water is easily taken into a non-aqueous ink composition containing the compound. Therefore, when a normal phthalocyanine derivative is used as the pigment dispersant, the generation of foreign matters due to the phthalocyanine derivative becomes particularly significant. In order to solve such a problem, the non-aqueous ink composition according to the present embodiment uses a phthalocyanine derivative having a specific structure. Therefore, even when the compound represented by the general formula (1) is contained, the generation of foreign matters is generated. Can be effectively suppressed. As a result, the non-aqueous ink composition according to the present embodiment is excellent in storage stability and can record an image excellent in abrasion resistance.

In the formula (1), R ¹ is preferably a methyl group or an n-butyl group. Thereby, the abrasion resistance and surface dryness of the image may be further improved.

  The HLB value of the compound represented by the formula (1) is preferably 8.0 or more and 20.0 or less, more preferably 8.5 or more and 18.5 or less, and more preferably 12.0 or more and 18. Particularly preferred is 5 or less. When the HLB value of the compound represented by the formula (1) is within the above range, it is more preferable in terms of interaction with the vinyl chloride resin. In addition, the HLB value in this specification is the following formula (i) from the ratio of the nonpolar value (I) and the organic value (O) in the organic conceptual diagram (hereinafter also simply referred to as “I / O value”). Is a value calculated by

  HLB value = (Nonpolar value (I) / Organic value (O)) × 10 (i)

  Specifically, I / O values are written by Atsushi Fujita, “Systematic Organic Qualitative Analysis Mixture”, Kazama Shobo, 1974; Norihiko Kuroki, “Dyeing Theoretical Chemistry”, Sakai Shoten, 1966; Hiroo Inoue , “Organic Compound Separation Method”, Suikabo, 1990.

The content of the compound represented by the general formula (1) is the total mass (100 of the non-aqueous ink composition).
% By mass) is preferably 5% by mass to 50% by mass, more preferably 5% by mass to 40% by mass, and still more preferably 5% by mass to 35% by mass. . When the content of the compound represented by the general formula (1) is 5% by mass or more, the abrasion resistance and surface drying property of the image can be further improved, and when the content is 50% by mass or less, the copper phthalocyanine derivative It is possible to further suppress the generation of aggregates due to the above.

1.2.2. Alkylene glycol monoalkyl ether The non-aqueous ink composition according to this embodiment preferably contains an alkylene glycol monoalkyl ether. The alkylene glycol monoalkyl ether has a function of improving the wet-spreading property of the ink, and particularly effectively acts on a recording medium with low ink absorption. As a result, the dot diameter of the droplets attached to the recording medium can be increased and an image with excellent glossiness can be recorded, so that the image quality of the obtained image is improved. In particular, by using an alkylene glycol monoalkyl ether and the compound represented by the general formula (1) in combination, an image having both image quality and abrasion resistance can be recorded.

  Examples of the alkylene glycol monoalkyl ether include ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monoisopropyl ether, ethylene glycol monobutyl ether, ethylene glycol monohexyl ether, ethylene glycol monophenyl ether, diethylene glycol monomethyl ether, diethylene glycol mono Ethyl ether, diethylene glycol monobutyl ether, diethylene glycol monohexyl ether, triethylene glycol monomethyl ether, triethylene glycol monoethyl ether, triethylene glycol monobutyl ether, tetraethylene glycol monomethyl ether, tetraethylene glycol monoethyl ether Ether, tetraethylene glycol monobutyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, dipropylene glycol monomethyl ether, dipropylene glycol monoethyl ether and the like. These compounds may be used alone or in combination of two or more. Among these, the standard boiling point is 280 ° C. because the wettability of the ink and the glossiness of the recorded image are improved, the drying property of the image is improved, and the occurrence of uneven printing of the image can be suppressed. It is preferable to use an alkylene glycol monoalkyl ether of the following (preferably 120 ° C. or higher and 280 ° C. or lower).

  When the alkylene glycol monoalkyl ether is contained, the content is preferably 1% by mass or more and 40% by mass or less with respect to the total mass (100% by mass) of the non-aqueous ink composition. % To 35% by mass is more preferable. When the content of the alkylene glycol monoalkyl ether is 1% by mass or more, the wettability of the ink and the glossiness of the image tend to be further improved, and when the content is 40% by mass or less, It tends to improve the drying property and suppress the occurrence of uneven printing.

1.2.3. Organic solvent other than the above The non-aqueous ink composition according to this embodiment contains an organic solvent other than the above (that is, an organic solvent other than the compound represented by the general formula (1) and the alkylene glycol monoalkyl ether). May be. Specific examples of organic solvents other than the above include glycol ethers (excluding the above-mentioned alkylene glycol monoalkyl ethers. For example, alkylene glycol dialkyl ethers), lactones (eg γ-butyrolactone, etc.), alcohols (eg, Ethyl alcohol, 1-propanol, fluorinated alcohol, etc.), ethers (eg, diethyl ether, dipropyl ether, etc.) and the like.

  When an organic solvent other than the above is contained, the content can be set to, for example, 5% by mass to 30% by mass with respect to the total mass (100% by mass) of the non-aqueous ink composition.

1.3. Pigment dispersant 1.3.1. Phthalocyanine derivative having a specific structure The non-aqueous ink composition according to this embodiment contains a phthalocyanine derivative into which a polar group having no amine structure is introduced as a pigment dispersant. In this specification, “a phthalocyanine derivative having a polar group having no amine structure introduced” may be referred to as “a phthalocyanine derivative having a specific structure”.

  The phthalocyanine derivative having a specific structure is a so-called pigment derivative (synergist). The pigment derivative has a function of improving the dispersibility of the pigment by adsorbing to the pigment or existing in the vicinity of the pigment. Thereby, the viscosity change etc. resulting from the fall of the dispersibility of a pigment can be suppressed favorably.

  The phthalocyanine derivative having a specific structure exhibits a property of being excellent in solubility in water by the action of a polar group having no amine structure introduced therein. Therefore, even if the amount of water in the ink is increased by the compound represented by the general formula (1), the phthalocyanine derivative having a specific structure is well dissolved in water, so that the generation of foreign matters can be reduced. In this way, by using a phthalocyanine derivative having a specific structure, an ink excellent in storage stability with little generation of foreign substances and less change in viscosity can be obtained.

Here, the “polar group having an amine structure” means a quaternary ammonium group (—N ⁺ R ¹ R ² R ³ X ⁻ ), an amino group (—NH ₂ , —NHR ⁴ , —NR ⁴ R ⁵ ). A group having an amine skeleton and an atom other than a nitrogen atom constituting the amine skeleton bonded to phthalocyanine (for example, —CONHR ⁶ , —SO ₂ NHR ⁶ , —OCONHR ⁶ , —CONHCOR ⁶ , —CONHSO ₂ R ^6, etc.) ) And the like. R ¹ , R ² , and R ³ each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or the like, and X ⁻ represents a counter ion. R ⁴ and R ⁵ each independently represents a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or the like. R ⁶ represents a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or the like. Examples of the substituent when the alkyl group and the aryl group are substituted include a sulfonic acid group, a carboxyl group, and a hydroxyl group.

  The “polar group not having an amine structure” refers to a group other than the polar group having the amine structure, and examples thereof include a sulfonic acid group and a carboxyl group. These exemplified polar groups are preferably used from the viewpoint that particularly excellent hydrophilicity can be imparted to the phthalocyanine derivative. Among the polar groups not having the amine structure exemplified above, a sulfonic acid group is preferable in that the solubility of the phthalocyanine derivative in water can be further improved.

  In addition, as the phthalocyanine derivative having a specific structure, it is preferable to use a phthalocyanine derivative that forms a complex with a metal from the viewpoint of excellent color developability. Among the phthalocyanine derivatives that form a complex with such a metal, a copper phthalocyanine derivative having copper as a central metal can be more preferably used.

When two or more polar groups are introduced per molecule of a phthalocyanine derivative having a specific structure, one or more of the introduced polar groups are polar groups having no amine structure, and 50% or more ( For example, when 10 polar groups are introduced, 5 or more are preferably polar groups having no amine structure, and 70% or more (for example, when 10 polar groups are introduced) Is more preferably a polar group having no amine structure, and 90% or more (for example, 9 or more when 10 polar groups are introduced) does not have an amine structure. Particularly preferred is a polar group. As a result, the phthalocyanine derivative having a specific structure is less likely to become a foreign substance in the ink.

  Commercially available products can be used for the phthalocyanine derivative having a specific structure, and examples thereof include Solsperse 12000 (trade name, manufactured by LUBRIZOL).

  The content of the phthalocyanine derivative having a specific structure is preferably 1 part by mass or more and 20 parts by mass or less, more preferably 1 part by mass or more and 10 parts by mass or less with respect to 100 parts by mass of the pigment described above. More preferably, it is at least 8 parts by mass. When the content of the phthalocyanine derivative having a specific structure is 1 part by mass or more, the dispersibility of the pigment can be further improved, and when the content is 20 parts by mass or less, the generation of foreign substances caused by the phthalocyanine derivative can be further suppressed. it can.

1.3.2. Other Pigment Dispersants The non-aqueous ink composition according to this embodiment preferably contains a pigment dispersant other than a phthalocyanine derivative having a specific structure. Examples of the pigment dispersant other than the phthalocyanine derivative having such a specific structure include a resin dispersant.

  The resin dispersant can further improve the dispersibility of the pigment due to a synergistic effect with the phthalocyanine derivative having the specific structure.

  Examples of the resin dispersant include polyvinyl alcohols, polyacrylic acid, acrylic acid-acrylonitrile copolymer, vinyl acetate-acrylic acid ester copolymer, acrylic acid-acrylic acid ester copolymer, and styrene-acrylic acid copolymer. Styrene-methacrylic acid copolymer, styrene-methacrylic acid-acrylic acid ester copolymer, styrene-α-methylstyrene-acrylic acid copolymer, styrene-α-methylstyrene-acrylic acid-acrylic acid ester copolymer Styrene-maleic acid copolymer, styrene-maleic anhydride copolymer, vinyl naphthalene-acrylic acid copolymer, vinyl naphthalene-maleic acid copolymer, vinyl acetate-maleic acid ester copolymer, vinyl acetate-croton Acid copolymers, vinyl acetate-acrylic acid copolymers, and the like Of the salt. Among these, a copolymer of a monomer having a hydrophobic functional group and a monomer having a hydrophilic functional group, and a polymer composed of a monomer having both a hydrophobic functional group and a hydrophilic functional group are preferable. As the form of the copolymer, any form of a random copolymer, a block copolymer, an alternating copolymer, and a graft copolymer can be used.

  Commercially available products can be used as the resin dispersant, such as Hinoact KF1-M, T-6000, T-7000, T-8000, T-8350P, T-8000E (all manufactured by Takefu Fine Chemical Co., Ltd.), etc. Polyester polymer compound, Solsperse 20000, 24000, 32000, 32500, 33500, 34000, 35200, 37500 (all manufactured by LUBRIZOL), Disperbyk-161, 162, 163, 164, 166, 180, 190, 191, 192, 2091, 2095 (both made by Big Chemie Japan), Floren DOPA-17, 22, 33, G-700 (both made by Kyoeisha Chemical Co., Ltd.), Addisper PB821, PB711 (both made by Ajinomoto Co., Inc.), LP40 0, LP4050, LP4055, POLYMER400,401,402,403,450,451,453 (all manufactured by EFKA Chemicals Co., Ltd.).

  When the resin dispersant is contained, the content thereof is preferably 5 parts by mass or more and 200 parts by mass or less, and more preferably 30 parts by mass or more and 120 parts by mass or less with respect to 100 parts by mass of the pigment. .

1.4. Resin The non-aqueous ink composition according to this embodiment preferably contains a resin. The function of the resin includes forming a film to improve the abrasion resistance of the image obtained from the non-aqueous ink composition. Such a resin is sometimes called a fixing resin.

  Examples of the resin include (meth) acrylic resin, vinyl chloride resin, aliphatic polyester, aromatic polyester, polyurethane, epoxy resin, polyvinyl acetate, ethylene-vinyl acetate copolymer resin, polycarbonate, polyvinyl butyral, polyvinyl alcohol. , Phenoxy resin, ethyl cellulose resin, cellulose acetate propionate resin, cellulose acetate butyrate, nitrocellulose resin, polystyrene, vinyltoluene-α-methylstyrene copolymer resin, polyamide, polyimide, polysulfone resin, petroleum resin, chlorination Examples thereof include polypropylene, polyolefin, terpene resin, rosin-modified phenol resin, various synthetic rubbers such as NBR / SBR / MBR, and modified products thereof. These resins may be used alone or in combination of two or more.

  Among the above resins, it is preferable to use at least one of a (meth) acrylic resin and a vinyl chloride resin from the viewpoint of further improving the abrasion resistance of the image. In particular, the combined use of a (meth) acrylic resin and a vinyl chloride resin tends to further improve the abrasion resistance of the recorded image.

  The (meth) acrylic resin is a polymer obtained from conventionally known monomer components. Such monomer components include, for example, acrylic esters such as methyl acrylate, ethyl acrylate, isopropyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate, methacrylic acid. Methacrylic acid esters such as isopropyl, n-butyl methacrylate, isobutyl methacrylate, tert-butyl methacrylate, cyclohexyl methacrylate, 2-ethylhexyl methacrylate, acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, maleic acid In addition to carboxyl group-containing monomers such as mono-n-butyl acid, mono-n-butyl fumarate, and mono-n-butyl itaconate, hydroxyl group-containing (meth) acrylic acid esters, amide group-containing monomers, glycidyl group-containing monomers , A cyano group-containing monomer, a hydroxyl group-containing allyl compound, a tertiary amino group-containing monomer, an alkoxysilyl group-containing monomer, or the like can be used alone or in combination. In the present invention, (meth) acrylic acid means both acrylic acid and methacrylic acid, and (meth) acrylate means both acrylate and methacrylate.

  Commercially available products may be used for the above (meth) acrylic resin. For example, Acrypet MF (trade name, manufactured by Mitsubishi Rayon Co., Ltd., acrylic resin), Sumipex LG (trade name, manufactured by Sumitomo Chemical Co., Ltd., acrylic resin) ), Paraloid B series (trade name, manufactured by Rohm and Haas, acrylic resin), Parapet G-1000P (trade name, manufactured by Kuraray Co., Ltd.), and the like.

  The vinyl chloride resin contains at least vinyl chloride as a monomer component used during the synthesis of the resin, and includes vinyl chloride and other monomers (for example, vinyl acetate, vinylidene chloride, acrylic, maleic acid, vinyl alcohol, etc.) These copolymers can be used. Among these, it is preferable to use a vinyl chloride-vinyl acetate copolymer obtained by copolymerizing vinyl chloride and vinyl acetate, and vinyl chloride-vinyl acetate having a glass transition temperature (Tg) of 60 ° C. or higher and 80 ° C. or lower. It is more preferable to use a copolymer.

Commercially available products may be used as the above-mentioned vinyl chloride resin, such as Kane Vinyl HM515, S-400 (trade name, manufactured by Kaneka Corporation), Solvain C (trade name, Nisshin Chemical Co., Ltd.), and the like. Can be mentioned.

  As the resin contained in the non-aqueous ink composition, any type of resin such as solid, solution, or emulsion may be used.

  The content of the resin in terms of solid content is preferably 0.5% by mass or more and 10% by mass or less with respect to the total mass (100% by mass) of the non-aqueous ink composition. The upper limit is more preferably 6% by mass or less, and further preferably 5% by mass or less. The lower limit is more preferably 1% by mass or more, and further preferably 2% by mass or more. By setting the resin content to 0.5% by mass or more, the abrasion resistance of the image tends to be further improved. Further, by setting the resin content to 10% by mass or less, the viscosity of the ink can be easily set in a range suitable for inkjet recording. Further, the smaller the resin content while ensuring the image's abrasion resistance, the more other components such as an organic solvent can be contained, which is preferable in terms of increasing the degree of design freedom.

1.5. Surfactant The non-aqueous ink composition according to this embodiment may contain a surfactant from the viewpoint of reducing the surface tension and improving the wet spreading property on the recording medium. Examples of the surfactant include a silicon-based surfactant, a fluorine-based surfactant, or a polyoxyethylene derivative that is a nonionic surfactant.

  As the silicon surfactant, it is preferable to use polyester-modified silicon or polyether-modified silicon. Specific examples include BYK-347, 348, BYK-UV3500, 3510, 3530, 3570 (all manufactured by Big Chemie Japan).

  As the fluorine-based surfactant, a fluorine-modified polymer is preferably used, and specific examples thereof include BYK-340 (manufactured by BYK Japan).

  As the polyoxyethylene derivative, it is preferable to use an acetylene glycol surfactant. Specific examples include Surfinol 82, 104, 465, 485, TG (all manufactured by Air Products Japan), Olphine STG, E1010 (all manufactured by Nissin Chemical Co., Ltd.), Nissan Nonion A-10R, A-13R. (All manufactured by NOF Corporation), Floren TG-740W, D-90 (manufactured by Kyoeisha Chemical Co., Ltd.), Neugen CX-100 (manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) and the like.

  When the surfactant is contained, the content thereof can be 0.1% by mass or more and 5% by mass or less with respect to the total mass (100% by mass) of the non-aqueous ink composition.

1.6. Other Components In addition to the above components, the non-aqueous ink composition according to this embodiment includes amines, various salts, a polymerizable compound, a pH adjuster, a chelating agent, an antiseptic / antifungal agent, and an anti-proofing agent. A substance for imparting a predetermined performance such as a rusting agent can be contained.

1.7. Preparation of Non-Aqueous Ink Composition The non-aqueous ink composition according to this embodiment has a surface tension at 20 ° C. of 20 mN / m or more and 50 mN / m from the viewpoint of the balance between recording quality and reliability as an ink for inkjet recording. m is preferable, and 25 mN / m or more and 40 mN / m or less is more preferable. The surface tension is measured by using an automatic surface tension meter CBVP-Z (manufactured by Kyowa Interface Science Co., Ltd.) by confirming the surface tension when the platinum plate is wetted with ink in an environment of 20 ° C. be able to.

  From the same viewpoint, the viscosity at 20 ° C. of the non-aqueous ink composition is preferably 2 mPa · s or more and 15 mPa · s or less, and more preferably 2 mPa · s or more and 10 mPa · s or less. The viscosity is measured by using a viscoelasticity tester MCR-300 (manufactured by Pysica), increasing the Shear Rate to 10 to 1000 in an environment of 20 ° C., and reading the viscosity at Shear Rate 200. Can be measured.

1.8. Physical Properties of Non-Aqueous Ink Composition The non-aqueous ink composition according to the present embodiment can be obtained by mixing the components described above in an arbitrary order and removing impurities by filtering or the like as necessary. As a method for mixing the components, a method in which materials are sequentially added to a container equipped with a stirring device such as a mechanical stirrer or a magnetic stirrer and stirred and mixed is suitably used. As a filtration method, centrifugal filtration, filter filtration, or the like can be performed as necessary.

2. Inkjet Recording Method An inkjet recording method according to an embodiment of the present invention includes a step of ejecting droplets of the non-aqueous ink composition from a recording head and adhering the droplets to a recording medium (hereinafter referred to as “step (a)”). Say). Thereby, a recorded matter having an image formed on the recording medium is obtained.

  According to the ink jet recording method according to the present embodiment, since the above non-aqueous ink composition is used, it is possible to record an image having excellent ink ejection properties and less fixability due to less generation of foreign matter. .

  In the ink jet recording method according to this embodiment, the step (a) is preferably performed on a recording medium heated to 30 ° C. or higher and 50 ° C. or lower. The ink drying property can be improved by adhering the ink composition described above to the heated recording medium.

  Further, the ink jet recording method according to the present embodiment may include post-heating (hereinafter referred to as “step (b)”) for further heating the recording medium after the step (a). Good. By further providing the step (b), the drying property of the ink can be further improved.

  As an ink jet recording apparatus that can include the steps as described above, any apparatus can be used in which the ink composition described above is ejected as droplets from fine nozzles of a recording head and the droplets are attached to a recording medium. be able to. Hereinafter, an ink jet printer having a mechanism capable of heating a recording medium will be described as an example of an ink jet recording apparatus usable in the present embodiment.

  FIG. 1 is a perspective view showing a configuration of an ink jet printer (hereinafter simply referred to as “printer”) that can be used in the present embodiment. The printer 1 shown in FIG. 1 is a so-called serial printer. A serial printer is a printer in which a recording head is mounted on a carriage that moves in a predetermined direction, and droplets are ejected onto a recording medium when the recording head moves as the carriage moves.

As shown in FIG. 1, a printer 1 includes a carriage 4 on which a recording head 2 is mounted and an ink cartridge 3 is detachably mounted; a platen 5 that is disposed below the recording head 2 and that transports a recording medium P; And a heating mechanism 6 for heating the recording medium, a carriage moving mechanism 7 for moving the carriage 4 in the medium width direction of the recording medium P, and a medium feeding mechanism 8 for conveying the recording medium P in the medium feeding direction. Is. The printer 1 also has a control device CONT that controls the operation of the entire printer 1. The medium width direction is the main scanning direction (head scanning direction). The medium feeding direction is a sub-scanning direction (a direction orthogonal to the main scanning direction).

  The ink cartridge 3 is composed of four independent cartridges. Each of the four cartridges is filled with the non-aqueous ink composition described above. In the example of FIG. 1, the number of cartridges is four. However, the number of cartridges is not limited to this, and a desired number of cartridges can be mounted.

  The ink cartridge 3 is not limited to the one mounted on the carriage 4 as shown in FIG. 1, but instead is one of the type that is mounted on the housing side of the printer 1 and supplied to the head 2 via the ink supply tube. There may be.

  The carriage 4 is attached in a state of being supported by a guide rod 9 which is a support member installed in the main scanning direction. The carriage 4 is moved in the main scanning direction along the guide rod 9 by the carriage moving mechanism 7. In the example of FIG. 1, the carriage 4 moves in the main scanning direction. However, the present invention is not limited to this, and the carriage 4 may move in the sub scanning direction in addition to the movement in the main scanning direction. .

  As long as the heating mechanism 6 is provided at a position where the recording medium P can be heated, the installation position is not particularly limited. In the example of FIG. 1, the heating mechanism 6 is installed on the platen 5 at a position facing the head 2. Thus, when the heating mechanism 6 is installed at a position facing the head 2, the adhesion position of the droplets on the recording medium P can be reliably heated, so that the droplets adhering to the recording medium P can be efficiently dried. it can.

  The heating mechanism 6 includes, for example, a print heater mechanism that heats the recording medium P in contact with a heat source, a mechanism that irradiates infrared rays or microwaves (electromagnetic waves having a maximum wavelength of about 2,450 MHz), and warm air. A dryer mechanism or the like for spraying can be used.

  The heating of the recording medium P by the heating mechanism 6 is performed before or when the droplets ejected from the nozzle holes (not shown) adhere to the recording medium P. In this way, the droplets attached to the recording medium P can be quickly dried. Control of various heating conditions (for example, heating timing, heating temperature, heating time, etc.) is performed by the control device CONT.

  The heating of the recording medium P by the heating mechanism 6 may be performed so that the recording medium P maintains a temperature range of 30 ° C. or more and 50 ° C. or less from the viewpoint of improving the drying property of the ink and preventing the deformation of the recording medium. preferable. In the present invention, the temperature at which the recording medium is heated means the temperature of the recording surface of the recording medium during heating.

  The printer 1 may further have a second heating mechanism (not shown) in addition to the heating mechanism 6. Since the printer 1 includes the second heating mechanism, the above-described step (b) can be performed by the printer 1. The second heating mechanism is installed downstream of the heating mechanism 6 in the conveyance direction of the recording medium P. The second heating mechanism heats the recording medium P after the recording medium P is heated by the heating mechanism 6, that is, after the droplets discharged from the nozzle holes (not shown) adhere to the recording medium P. Is what you do. Thereby, the drying property of the droplets of the ink composition adhering to the recording medium P can be further improved. Any of the mechanisms described in the heating mechanism 6 (for example, a dryer mechanism) can be used as the second heating mechanism.

The recording medium P is preferably heated by the second heating mechanism so that the recording medium P maintains a temperature range of 30 ° C. or more and 50 ° C. or less for the same reason as the heating mechanism 6.

  The linear encoder 10 detects the position of the carriage 4 in the main scanning direction with a signal. This detected signal is transmitted to the control device CONT as position information. The control device CONT recognizes the scanning position of the recording head 2 based on the position information from the linear encoder 10, and controls the recording operation (discharge operation) by the recording head 2. Further, the control device CONT is configured to be able to variably control the moving speed of the carriage 4.

The recording medium P is not particularly limited, but according to the ink jet recording method according to the present embodiment, the recorded image has good abrasion resistance and dryness even when a low-absorbency recording medium is used. Become. Here, the “low absorption recording medium” refers to a recording medium having a water absorption amount of 10 mL / m ² or less from the start of contact to 30 msec ^1/2 in the Bristow method. What is necessary is just to have a property. According to this definition, the “low absorption recording medium” in the present invention includes a non-absorbing recording medium that does not absorb water at all. This Bristow method is the most popular method for measuring the amount of liquid absorbed in a short time, and is also adopted by the Japan Paper Pulp Technology Association (JAPAN TAPPI). For details of the test method, refer to Standard No. of “JAPAN TAPPI Paper Pulp Test Method 2000”. 51 "Paper and paperboard-Liquid absorbency test method-Bristow method".

  Specific examples of the low-absorbency recording medium include sheets, films, and textile products containing a low-absorbency material. The low-absorbency recording medium is a layer containing a low-absorbency material (hereinafter referred to as “low-absorbency layer”) on the surface of a substrate (for example, paper, fiber, leather, plastic, glass, ceramics, metal, etc.). May also be provided. Although it does not specifically limit as a low absorptive material, Olefin resin, ester resin, urethane resin, acrylic resin, vinyl chloride resin etc. are mentioned.

  Among these, as the low-absorbency recording medium, one having a recording surface containing a vinyl chloride resin can be preferably used. The non-aqueous ink composition described above contains the compound represented by the general formula (1), and this compound dissolves the recording surface containing the vinyl chloride resin, so that the ink composition is placed inside the recording medium. Can penetrate. Thereby, the abrasion resistance of images and characters recorded on the recording surface containing the vinyl chloride resin can be further improved. Specific examples of the vinyl chloride resin include polyvinyl chloride, vinyl chloride-ethylene copolymer, vinyl chloride-vinyl acetate copolymer, vinyl chloride-vinyl ether copolymer, vinyl chloride-vinylidene chloride copolymer, vinyl chloride. -Maleic acid ester copolymer, vinyl chloride- (meth) acrylic acid copolymer, vinyl chloride- (meth) acrylic acid ester copolymer, vinyl chloride-urethane copolymer and the like. Note that there are no particular restrictions on the various properties such as thickness, shape, color, softening temperature, and hardness of the low-absorbency recording medium.

3. EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples and comparative examples. However, the present invention is not limited only to these examples.

3.1. Synthesis of organic solvent 3.1.1. Compound represented by the following formula (2) Into a 300 ml separable flask equipped with a stirrer, a thermocouple and a nitrogen gas inlet tube, 19.828 g of N, N-dimethylacrylamide and 6.408 g of methanol were introduced, and nitrogen gas was introduced. While stirring. Next, 0.338 g of sodium t-butoxide was added and reacted at 35 ° C. for 4 hours. After completion of heating, 150 mg of phosphoric acid was added to make the solution uniform, and the mixture was allowed to stand for 3 hours. The solution was filtered to remove precipitates, and unreacted substances were removed with an evaporator. In this way, a compound represented by the following formula (2) (hereinafter also referred to as “organic solvent A”) was obtained.

  In addition, the HLB value calculated by the said Formula (i) from the I / O value in an organic conceptual diagram of the obtained organic solvent A was 18.3.

3.1.2. Compound represented by the following formula (3) Into a 300 ml separable flask equipped with a stirrer, a thermocouple and a nitrogen gas introduction tube, 19.828 g of N, N-dimethylacrylamide and 14.824 g of 1-butanol were added, and nitrogen gas was added. Was stirred while being introduced. Next, 0.338 g of sodium t-butoxide was added and reacted at 35 ° C. for 4 hours. After completion of heating, 150 mg of phosphoric acid was added to make the solution uniform, and the mixture was allowed to stand for 3 hours. The solution was filtered to remove precipitates, and unreacted substances were removed with an evaporator. In this way, a compound represented by the following formula (3) (hereinafter also referred to as “organic solvent B”) was obtained.

  In addition, the HLB value calculated by the said Formula (3) from the I / O value in an organic conceptual diagram of the obtained organic solvent B was 12.2.

3.2. Preparation of non-aqueous ink composition Only an organic solvent in an amount corresponding to the concentration shown in Table 1 was stirred in each container for each ink to obtain a mixed solvent. Part of the obtained mixed solvent was separated, and a predetermined amount of Solsperse 12000 or Solsperse 5000 (both trade names manufactured by LUBRIZOL), Solsperse 37500 (trade name, manufactured by LUBRIZOL), and a pigment were added, and a homogenizer was added. After preliminarily dispersing using, a pigment dispersion having an average particle diameter of 130 nm of pigment was obtained by performing a dispersion treatment in a bead mill filled with zirconia beads having a diameter of 0.3 mm. Then, a resin solution was obtained by adding a resin to what had been mixed with a part of the mixed solvent, followed by stirring to obtain a completely dissolved resin solution. The above pigment dispersant is mixed with the remainder of the mixed solvent, the surfactant and the above resin solution, stirred for 1 hour, and then filtered using a 5 μm PTFE membrane filter. A non-aqueous ink composition according to an example was obtained.

Of the components used in the table, the components described by trade names or abbreviations are as follows.
・ PB-7 (CI Pigment Black 7, Carbon Black)
・ Solsperse 37500 (trade name, manufactured by LUBRIZOL, resin dispersant)
Solsperse 12000 (trade name, manufactured by LUBRIZOL, a copper phthalocyanine derivative having a sulfonic acid group introduced)
・ Solsperse 5000 (trade name, manufactured by LUBRIZOL, copper phthalocyanine derivative with ammonium salt introduced)
Organic solvent A (compound represented by the above formula (2))
Organic solvent B (compound represented by the above formula (3))
DPGmME (dipropylene glycol monomethyl ether, standard boiling point 187 ° C.)
TetraEGmBE (tetraethylene glycol monobutyl ether, standard boiling point 300 ° C.)
DEGdEE (diethylene glycol diethyl ether, standard boiling point 189 ° C.)
・ BYK340 (trade name, manufactured by BYK Japan, fluorinated surfactant)
HM515 (trade name “Kane Vinyl HM515”, manufactured by Kaneka Corporation, vinyl chloride-vinyl acetate copolymer)
・ G-1000P (trade name “Parapet G-1000P”, methacrylic resin)

3.3. Evaluation Test Among the evaluation tests, evaluation of printing unevenness, gloss, dot size, and friction fastness was performed under the following conditions. Using an air conditioner and a humidifier, the temperature and humidity of the environmental test room are adjusted to 25 ° C. and 65% RH, respectively, and an ink jet printer “SC” manufactured by Seiko Epson Corporation installed in the environmental test room. -S30650 "(trade name). The temperature and humidity were measured by a temperature / humidity sensor installed on a housing that was not affected by the heat generated by the inkjet printer itself such as a heater.

  In each evaluation test, the recording medium was heated at 45 ° C. during the recording and for 1 minute after the recording in the platen and the recording medium discharge portion downstream from the platen.

3.3.1. Ink storage stability (viscosity change and generation of foreign matter)
Each non-aqueous ink composition was filled in an ink cartridge for Seiko Epson printer SC-S30650 and left in an environment of 60 ° C. and 80% for 2 weeks. Thereafter, the ink was taken out, and the viscosity when the temperature of the ink was 20 ° C. was measured with a viscometer (trade name “MCR300”) manufactured by Anton Paar. The level at which the amount of change from the initial viscosity (the temperature of the ink at the time of measurement of 20 ° C.) was 0.1 mPa · s or more was judged as x, and the level less than 0.1 mPa · s was judged as ◯.

  In addition, the presence or absence of foreign matter in the ink after standing was observed with an electron microscope, and the presence or absence of foreign matter derived from the copper phthalocyanine derivative was confirmed.

3.3.2. Printing unevenness After printing each non-aqueous ink composition on a vinyl chloride banner sheet (manufactured by 3M, model number IJ51 (polyvinyl chloride)) at a 100% concentration with a recording resolution of 720 × 720 dpi, 60 It was dried for 25 minutes at 25 ° C. and 65% RH (relative humidity). Thereafter, the printed surface was observed visually and using an optical microscope, and 6 points with little printing unevenness were evaluated to 6 points up to 1 point.

3.3.3. Glossiness After printing each non-aqueous ink composition on a glossy polyvinyl chloride sheet (Roland DG, model number SV-G-1270G) at a 100% density with a recording resolution of 720 × 720 dpi using the above printer, A recorded matter was prepared by drying at 25 ° C. and 65% RH (relative humidity) for 1 day. Then, the 20 ° gloss of the solid printing part is measured with MULTI GLOSS 268 (manufactured by Konica Minolta Co., Ltd.), and the glossiness is less than 26 at one point and between 26 and less than 28 is 2
The gloss was scored by scoring the glossiness every 2 points. When the gloss is excellent, there is an advantage that the same glossiness as that of the recording medium itself can be obtained on the recorded matter particularly in a recording medium having gloss such as a film.

3.3.4. Dot size Using the above printer, print each non-aqueous ink composition on a PVC banner sheet (manufactured by 3M, model number IJ51 (polyvinyl chloride)) with a 30% recording resolution of 720 x 720 dpi and a 3 cm square on each side. And then dried at 25 ° C. and 65% RH (relative humidity) for 60 minutes. Then, the dot size of the printing part was observed using the optical microscope, and the dot diameter was classified every 10 μm. When the blur was large, the dot shape was not circular and measurement was not possible. Moreover, although it became close to a perfect circle due to small blurring, the dot size (diameter) was small. The score was calculated by ranking every 10 μm, with a dot size of 20 μm or less as one point and a dot size exceeding 20 μm and 30 μm or less being two points. A good dot size means that the ink spreads well on the recording medium, and that the recording medium can be covered with ink, so that the color development of the recorded matter is improved. .

3.3.5. Friction Fastness After printing each non-aqueous ink composition on a glossy polyvinyl chloride sheet (Roland DG, model number SV-G-1270G) using the above printer at a recording resolution of 720 × 720 dpi, 100% density, A recorded matter was prepared by drying at 25 ° C. and 65% RH (relative humidity) for 1 day. Next, based on JIS L 0849, the dry type test was done with the I type testing machine. Thereafter, the OD of the test cotton fabric was measured with a Spectrolino (manufactured by Gretag Macbeth Co., Ltd.). A score was given for the transfer.

3.4. Evaluation results Table 1 shows the results of the above evaluation tests.

  All of the non-aqueous ink compositions according to the examples were found to be less likely to generate foreign matter and change in viscosity (that is, excellent in storage stability) and excellent in abrasion resistance of recorded images. In addition, since the content of the phthalocyanine derivative having a specific structure was within the range of 1 part by mass or more and 20 parts by mass or less with respect to 100 parts by mass of the pigment, all the non-aqueous ink compositions according to the examples were specified. Compared with a non-aqueous ink composition (not shown in the table) in which the content of the phthalocyanine derivative having the structure was out of the above range, the viscosity change was much smaller and the generation of foreign matters was more excellent.

  In addition, since the non-aqueous ink composition according to Example 7 did not contain alkylene glycol monoalkyl ether, it was shown that the dot size is insufficient and the image quality tends to deteriorate.

  On the other hand, since the non-aqueous ink composition according to Comparative Example 1 does not contain a pigment derivative, it has been shown that the viscosity change of the ink is large and the storage stability is not excellent.

  Since the ink composition according to Comparative Example 2 does not contain the compound represented by the general formula (1), it was shown that the abrasion resistance of the recorded image is lowered. In addition, the ink composition of Comparative Example 2 deteriorated the evaluation of printing unevenness because the drying property of the image was lowered as the content of the alkylene glycol monoalkyl ether was increased.

  Since the non-aqueous ink composition according to Comparative Example 3 did not use a phthalocyanine derivative having a specific structure as a pigment derivative but used a phthalocyanine derivative having an amine structure, the generation of foreign matters became significant.

  The present invention is not limited to the embodiments described above, and various modifications are possible. For example, the present invention includes substantially the same configuration (for example, a configuration having the same function, method, and result, or a configuration having the same purpose and effect) as the configuration described in the embodiment. In addition, the invention includes a configuration in which a non-essential part of the configuration described in the embodiment is replaced. In addition, the present invention includes a configuration that achieves the same effect as the configuration described in the embodiment or a configuration that can achieve the same object. In addition, the invention includes a configuration in which a known technique is added to the configuration described in the embodiment.

DESCRIPTION OF SYMBOLS 1 ... Printer, 2 ... Recording head, 3 ... Ink cartridge, 4 ... Carriage, 5 ... Platen, 6 ... Heating mechanism, 7 ... Carriage moving mechanism, 8 ... Medium feed mechanism, 9 ... Guide lot, 10 ... Linear encoder, P …recoding media

Claims (9)

Pigments,
A compound represented by the following general formula (1):
As a pigment dispersant for dispersing the pigment, a phthalocyanine derivative into which a polar group having no amine structure is introduced,
A non-aqueous ink composition for inkjet recording, comprising:

(In the general formula (1), R ¹ represents an alkyl group having 1 to 4 carbon atoms, and R ² and R ³ each independently represent a methyl group or an ethyl group.) In claim 1,
A non-aqueous ink composition for ink jet recording, wherein the pigment is carbon black. In claim 1 or claim 2,
Furthermore, the non-aqueous ink composition for inkjet recording containing alkylene glycol monoalkyl ether. In claim 3,
A non-aqueous ink composition for inkjet recording, wherein the content of the alkylene glycol monoalkyl ether is 1% by mass or more and 40% by mass or less based on the total mass of the non-aqueous ink composition. In any one of Claims 1 thru | or 4,
A non-aqueous ink composition for inkjet recording, wherein the content of the compound represented by the general formula (1) is 5% by mass or more and 50% by mass or less with respect to the total mass of the non-aqueous ink composition. In any one of Claims 1 thru | or 5,
Furthermore, the non-aqueous ink composition for inkjet recording containing at least one resin of a vinyl chloride resin and a (meth) acrylic resin. In claim 6,
A non-aqueous ink composition for ink jet recording, wherein the content of the resin is 0.5% by mass or more and 10% by mass or less with respect to the total mass of the non-aqueous ink composition. In any one of Claims 1 thru | or 7,
A non-aqueous ink composition for inkjet recording, wherein a content of the phthalocyanine derivative is 1 part by mass or more and 20 parts by mass or less with respect to 100 parts by mass of the pigment. In any one of Claims 1 thru | or 8,
A non-aqueous ink composition for inkjet recording, further comprising a compound other than the phthalocyanine derivative as the pigment dispersant.

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